Mondo Disease Ontology
5921 terms(s) returned
| Term Type: | Record: 2701 to 2750 of 5921 Records | Page: 55 of 119, First Previous Next Last | Show Records Per Page |
- Atelidae
- Atelinae
- Atelis syndrome
- Atelis syndrome 1
- Atelis syndrome 2
- Atherinomorphae
- Athrombia, essential
- Atkin-Flaitz syndrome
- Atlantoaxial abnormality
- Atlantoaxial dislocation
- Atresia of the Eustachian tube
- Atresia of the external auditory canal
- Atretic gallbladder
- Atrial septal defect
- Atrichia
- Atrioventricular block
- Atrioventricular valve regurgitation
- Atrophic pituitary gland
- Atrophy of alveolar ridges
- Atrophy/Degeneration affecting the brainstem
- Atrophy/Degeneration affecting the central nervous system
- Atrophy/Degeneration affecting the cerebrum
- Atrophy/Degeneration involving the spinal cord
- Atypical behavior
- Atypical scarring of skin
- Au-Kline syndrome
- Aureobasidium
- Australaves
- Autism
- Autistic behavior
- Autoimmunity
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- Avascular necrosis
- Aves
- Avian coronavirus
- Avulavirinae
- Avulavirus
- Avulavirus infectious disease
- Axenfeld anomaly
- Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
- Axenfeld-Rieger syndrome
- Axenfeld-Rieger syndrome type 1
- Axenfeld-Rieger syndrome type 2
- Axenfeld-Rieger syndrome type 3
- Axial hypotonia
- Axial muscle atrophy
- Axial muscle weakness
- Axillary apocrine gland hypoplasia
- Ayme-Gripp syndrome
